Malignant soft tissue lesions Flashcards

1
Q

Most important factor for limiting recurrence

A

margins

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2
Q

Soft tissue sarcomas that spread to regional lymph nodes

A

rhabdomyosarcoma, synovial sarcoma, clear cell sarcoma, epitheloid sarcoma, angiosarcoma

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3
Q

Most common sarcoma in lower extremities, young adult, cystic appearing with fluid levels, may have mineralization

A

Synovial sarcoma, mets to lung, Surgical excision and radiation

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4
Q

Translocation for synovial sarcoma

A

X:18, SYT SSX1 or 2 fusion protein

vimentin, keratin, EMA

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5
Q

Aggressive soft tissue lesion, often in retroperitoneum but moth eaten apearance to metaphysis of long bone, histo blunt cigar shaped nuclei with pink cytoplast

A

Leiomyosarcoma

wide excision and radiation chemo if lung mets

desmin/actin (muscle), +vimentin (sarcoma)

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6
Q

old person, chronic venous statis, overlying skin changes

A

angiosarcoma, tumor from endothelium of blood vessels

surgery and radiation

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7
Q

young adult with tumor in hand or forearm, nodular pattern with central necrosis, eosinophilic cytoplasm

A

epitheliod sarcoma, keratin +, wide resection and radiation

beware of lymph node spread

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8
Q

20-40 yo, usually associated with tendons on dorsum of foot, sheets of cells with clear cytoplasma and spindle cells

A

clear cell sarcoma, amputation and chemo

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9
Q

clear cell sarcoma translocation and staining

A

S-100, HMB-45

t(12;22) EWS AFT1, neuroectodermal

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10
Q

most common soft tissue sarcoma in children

A

rhabdomyosarcoma

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11
Q

Translocation for rhabdomyosarcoma

A

t(2:13) Pax3-FKHR

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12
Q

Treatment for rhabdomyosarcoma

A

chemo, resection, radiation

Lymph node spread common, must do bone marrow aspiration

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13
Q

Stains positive in rhabdomyosarcoma

A

vitemin, desmin/actin, myosin(MyoD1)

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14
Q

most common soft tissue sarcoma, middle aged, deep lesions in thigh or retroperitoneum

A

Liposarcoma

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15
Q

chromosomal translocation of myxoid liposarcoma

A

t(12;16) CHOP,TLS

MDM2

always order CT chest/ab/pelvis in myxoid

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16
Q

Types of liposarcoma

A

well-differentieated, myxoid, round cell, pleomorphic, undiff

17
Q

treatment for liposarcoma

A

resection and radiation

18
Q

Important prognostic factor in melanoma

A

depth

19
Q

Treatment of melanoma

A

<1mm local resection

> 1mm local resection with 1-2cm margin, sentinel node bx

20
Q

Tumor of brown fat

A

hibernoma

21
Q

Treatment of atypical liposarcoma

A

resection

22
Q

Patient with history of abdominal wall cancer, possible historyof FAP or Gardner syndrome, aggressive bubbly lesion if in bone

A

Desmoid tumor (fibromatosis), desmoplastic fibroma

usually around shoulder

dense spindlecellsin rows with elongated nuclei

23
Q

Treatment of desmoid tumor

A

NSAID, chemo, resection

tamoxifen if estrogen receptor positive

increased beta catenin (trisomy 8 or 20)

24
Q

Recurrent atraumatic hemoarthrosis, possible erosive changes on xrays, blooms on MRI

A

PVNS (tenosynovial giant cell)

hemosiderin in giant cells

focal nodular (simpe excision), extensive synovectomy plus radiation otherwise

Over expression of CSF-1 (pexidantinib)

25
Q

Middle aged patient with painful mass on finger tip, bluish color, nail ridging, sensitive

A

Glomus tumor (pain, tenderness, cold intolerance) - perivascular temp regulating structure

small round blue cells on histo

Marginal excision

26
Q

Middle aged patient with metaplastic changes in synovial tissue and chondroid loose bodies in the joint

A

Synovial chondromatosis (osteochondromatosis if mineralized on xray)

marbles in joint, histo shows hyaline cartilage

remove loose bodes and synovectomy